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  2. Henoch–Schönlein purpura - Wikipedia

    en.wikipedia.org/wiki/Henoch–Schönlein_purpura

    As of 2017, the optimal way to treat Henoch–Schönlein purpura remains controversial. [22] Analgesics may be needed for the abdominal and joint pains. Wound care is warranted if skin death and ulcerations occur. [22] It is uncertain as to whether HSP needs treatment beyond controlling the symptoms.

  3. Cryofibrinogenemia - Wikipedia

    en.wikipedia.org/wiki/Cryofibrinogenemia

    Cryofibrinogenemia refers to a condition classified as a fibrinogen disorder in which a person's blood plasma is allowed to cool substantially (i.e. from its normal temperature of 37 °C to the near-freezing temperature of 4 °C), causing the (reversible) precipitation of a complex containing fibrinogen, fibrin, fibronectin, and, occasionally, small amounts of fibrin split products, albumin ...

  4. List of ICD-9 codes 280–289: diseases of the blood and blood ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_280...

    289.50 Disease of spleen unspecified; 289.51 Chronic congestive splenomegaly; 289.52 Splenic sequestration; 289.53 Neutropenic splenomegaly; 289.59 Other diseases of spleen; 289.6 Familial polycythemia; 289.7 Methemoglobinemia; 289.8 Other specified diseases of blood and blood-forming organs 289.81 Primary hypercoagulable state; 289.82 ...

  5. Purpura - Wikipedia

    en.wikipedia.org/wiki/Purpura

    Purpura (/ ˈ p ɜːr p jʊər ə / [1]) is a condition of red or purple discolored spots on the skin that do not blanch on applying pressure. The spots are caused by bleeding underneath the skin secondary to platelet disorders, vascular disorders, coagulation disorders, or other causes. [ 2 ]

  6. Type III hypersensitivity - Wikipedia

    en.wikipedia.org/wiki/Type_III_hypersensitivity

    Immune complex glomerulonephritis, as seen in Henoch-Schönlein purpura; this is an example of IgA involvement in a nephropathy. The reaction can take hours, days, or even weeks to develop, depending on whether or not there is immunological memory of the precipitating antigen. Typically, clinical features emerge a week following initial antigen ...

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  8. Purpura fulminans - Wikipedia

    en.wikipedia.org/wiki/Purpura_fulminans

    Purpura fulminans is an acute, often fatal, thrombotic disorder which manifests as blood spots, bruising and discolouration of the skin resulting from coagulation in small blood vessels within the skin and rapidly leads to skin necrosis and disseminated intravascular coagulation.

  9. Palpable purpura - Wikipedia

    en.wikipedia.org/wiki/Palpable_purpura

    Inflammation-induced damage to the skin's blood vessels causes palpable purpura. Palpable purpura is the clinical manifestation of leukocytoclastic vasculitis, which can be idiopathic or linked to sepsis, reactions to drugs, connective tissue diseases, cryoglobulinemia, hepatitis C or B infection, or underlying cancers

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